meddevicedb.com FDA Device Reference

Tanning Lamp

K143043 Class II Traditional
Decision Date
2015-04-02
Sponsor / Applicant
Unilam Co., Ltd.

Technical Specification

510(k) Submission ID K143043
Product Code LEJ
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4635
Decision Date 2015-04-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Tanning Lamp received FDA 510(k) clearance under submission number K143043, sponsored by Unilam Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2015-04-02.

Classification & Regulation

This clearance is catalogued under FDA product code LEJ and 21 CFR 878.4635, within the General, Plastic Surgery review panel as a Class II device.